Medical Director, Medical Affairs – Neurology

🔥 0 minutes ago

🌐 Bulgaria, Poland, +3 more countries – Remote

🇧🇬 Bulgaria – Remote 🇵🇱 Poland – Remote 🇭🇷 Croatia – Remote 🇬🇧 United Kingdom – Remote 🇷🇴 Romania – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Serve as Global Lead Medical Monitor for assigned pan-regional and/or global trials • Provide therapeutic and protocol-specific training to project teams • Contribute medical input to clinical development programs, study protocols, research papers, and client-focused white papers • Maintain competence in assigned projects through internal meetings, therapeutic and clinical literature review, and conferences and meetings • Assist with annual departmental revenue targets and other activities directed by senior management • Review and/or assist in preparing final study reports, protocols, ISS/ISEs, and other study documentation • Support Business Development through proposals, feasibility assessments, medical-services proposal and contract reviews, and sponsor meetings • Mentor other medical staff as directed by senior management • Support senior management’s leadership of the department and company • Ensure compliance with ethical, legal, and regulatory standards

🎯 Requirements

• Medical degree (MD or internationally recognized equivalent) with specialization in Neurology required • Board certification in Neurology or internationally recognized equivalent required • 6-8 years in the CRO, Pharma or Biotech industry with the medical monitoring or study physician role • Valid passport and ability to travel if required • Working knowledge of GCPs and regulatory requirements relating to clinical development and safety • Experience reviewing and/or assisting in the preparation of final study reports (CSRs), protocols, ISS/ISEs, or other study documentation • Proven track record supporting Business Development through proposal generation, feasibility assessments, medical-services proposal/contract review, and sponsor meetings • Robust clinical/therapeutic acumen in medical subspecialty • Experience in pediatric neurology and/or gene therapy neurology is considered a significant advantage